Transcript #00026976 (NM_198994.2, TGM6 gene)

Transcript name transcript variant 1
Gene name TGM6 (transglutaminase 6)
Chromosome 20
Transcript - NCBI ID NM_198994.2
Transcript - Ensembl ID -
Protein - NCBI ID NP_945345.2
Protein - Ensembl ID -
Protein - Uniprot ID -
Remarks -
Date created 0000-00-00 00:00:00 +00:19 (LMT)
Date last edited N/A


Variants

177 entries on 2 pages. Showing entries 1 - 100.
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Affects function     

Exon     

AscendingDNA change (cDNA)     

Position     

RNA change     

Protein     

PolyPhen prediction     

GVS function     

Splice distance     
./. - c.-2A>G -2 r.(=) p.(=) - utr-5 -
./. - c.-2A>G -2 r.(=) p.(=) - utr-5 -
./. - c.-2A>G -2 r.(=) p.(=) - utr-5 -
./. - c.12C>G 12 r.(?) p.(Ile4Met) - missense -
./. - c.42G>A 42 r.(?) p.(=) - coding-synonymous -
./. - c.111G>A 111 r.(?) p.(=) - coding-synonymous -
./. - c.146A>T 146 r.(?) p.(Asp49Val) - missense -
./. - c.172A>G 172 r.(?) p.(Met58Val) - missense -
./. - c.172A>G 172 r.(?) p.(Met58Val) - missense -
./. - c.172A>G 172 r.(?) p.(Met58Val) - missense -
./. - c.172A>G 172 r.(?) p.(Met58Val) - missense -
./. - c.172A>G 172 r.(?) p.(Met58Val) - missense -
./. - c.172A>G 172 r.(?) p.(Met58Val) - missense -
./. - c.172A>G 172 r.(?) p.(Met58Val) - missense -
./. - c.172A>G 172 r.(?) p.(Met58Val) - missense -
./. - c.172A>G 172 r.(?) p.(Met58Val) - missense -
./. - c.172A>G 172 r.(?) p.(Met58Val) - missense -
./. - c.172A>G 172 r.(?) p.(Met58Val) - missense -
./. - c.172A>G 172 r.(?) p.(Met58Val) - missense -
./. - c.172A>G 172 r.(?) p.(Met58Val) - missense -
./. - c.172A>G 172 r.(?) p.(Met58Val) - missense -
./. - c.172A>G 172 r.(?) p.(Met58Val) - missense -
./. - c.172A>G 172 r.(?) p.(Met58Val) - missense -
./. - c.172A>G 172 r.(?) p.(Met58Val) - missense -
./. - c.172A>G 172 r.(?) p.(Met58Val) - missense -
./. - c.172A>G 172 r.(?) p.(Met58Val) - missense -
./. - c.172A>G 172 r.(?) p.(Met58Val) - missense -
./. - c.172A>G 172 r.(?) p.(Met58Val) - missense -
./. - c.172A>G 172 r.(?) p.(Met58Val) - missense -
./. - c.172A>G 172 r.(?) p.(Met58Val) - missense -
./. - c.172A>G 172 r.(?) p.(Met58Val) - missense -
./. - c.172A>G 172 r.(?) p.(Met58Val) - missense -
./. - c.172A>G 172 r.(?) p.(Met58Val) - missense -
./. - c.172A>G 172 r.(?) p.(Met58Val) - missense -
./. - c.172A>G 172 r.(?) p.(Met58Val) - missense -
./. - c.172A>G 172 r.(?) p.(Met58Val) - missense -
./. - c.172A>G 172 r.(?) p.(Met58Val) - missense -
./. - c.172A>G 172 r.(?) p.(Met58Val) - missense -
./. - c.422C>A 422 r.(?) p.(Ala141Glu) - missense-near-splice -
./. - c.422C>A 422 r.(?) p.(Ala141Glu) - missense-near-splice -
./. - c.430G>A 430 r.(?) p.(Asp144Asn) - missense -
./. - c.477C>T 477 r.(?) p.(=) - coding-synonymous -
./. - c.789G>A 789 r.(?) p.(=) - coding-synonymous -
./. - c.789G>A 789 r.(?) p.(=) - coding-synonymous -
./. - c.789G>A 789 r.(?) p.(=) - coding-synonymous -
./. - c.789G>A 789 r.(?) p.(=) - coding-synonymous -
./. - c.789G>A 789 r.(?) p.(=) - coding-synonymous -
./. - c.789G>A 789 r.(?) p.(=) - coding-synonymous -
./. - c.789G>A 789 r.(?) p.(=) - coding-synonymous -
./. - c.789G>A 789 r.(?) p.(=) - coding-synonymous -
./. - c.789G>A 789 r.(?) p.(=) - coding-synonymous -
./. - c.789G>A 789 r.(?) p.(=) - coding-synonymous -
./. - c.850+12G>A 850 r.(=) p.(=) - intron 12
./. - c.850+12G>A 850 r.(=) p.(=) - intron 12
./. - c.850+12G>A 850 r.(=) p.(=) - intron 12
./. - c.850+12G>A 850 r.(=) p.(=) - intron 12
./. - c.850+12G>A 850 r.(=) p.(=) - intron 12
./. - c.850+12G>A 850 r.(=) p.(=) - intron 12
./. - c.850+12G>A 850 r.(=) p.(=) - intron 12
./. - c.850+12G>A 850 r.(=) p.(=) - intron 12
./. - c.850+12G>A 850 r.(=) p.(=) - intron 12
./. - c.850+12G>A 850 r.(=) p.(=) - intron 12
./. - c.850+12G>A 850 r.(=) p.(=) - intron 12
./. - c.850+12G>A 850 r.(=) p.(=) - intron 12
./. - c.850+12G>A 850 r.(=) p.(=) - intron 12
./. - c.850+12G>A 850 r.(=) p.(=) - intron 12
./. - c.850+12G>A 850 r.(=) p.(=) - intron 12
./. - c.850+12G>A 850 r.(=) p.(=) - intron 12
./. - c.850+12G>A 850 r.(=) p.(=) - intron 12
./. - c.850+12G>A 850 r.(=) p.(=) - intron 12
./. - c.850+12G>A 850 r.(=) p.(=) - intron 12
./. - c.850+12G>A 850 r.(=) p.(=) - intron 12
./. - c.850+12G>A 850 r.(=) p.(=) - intron 12
./. - c.850+12G>A 850 r.(=) p.(=) - intron 12
./. - c.850+12G>A 850 r.(=) p.(=) - intron 12
./. - c.850+12G>A 850 r.(=) p.(=) - intron 12
./. - c.850+12G>A 850 r.(=) p.(=) - intron 12
./. - c.850+12G>A 850 r.(=) p.(=) - intron 12
./. - c.850+12G>A 850 r.(=) p.(=) - intron 12
./. - c.1093+5G>A 1093 r.spl? p.? - splice 5
./. - c.1093+5G>A 1093 r.spl? p.? - splice 5
./. - c.1093+5G>A 1093 r.spl? p.? - splice 5
./. - c.1093+5G>A 1093 r.spl? p.? - splice 5
./. - c.1093+5G>A 1093 r.spl? p.? - splice 5
./. - c.1093+5G>A 1093 r.spl? p.? - splice 5
./. - c.1093+5G>A 1093 r.spl? p.? - splice 5
./. - c.1093+5G>A 1093 r.spl? p.? - splice 5
./. - c.1093+5G>A 1093 r.spl? p.? - splice 5
./. - c.1108G>A 1108 r.(?) p.(Gly370Ser) - missense -
./. - c.1126G>A 1126 r.(?) p.(Ala376Thr) - missense -
./. - c.1171G>A 1171 r.(?) p.(Val391Met) - missense -
./. - c.1301G>A 1301 r.(?) p.(Arg434His) - missense -
./. - c.1476G>A 1476 r.(?) p.(=) - coding-synonymous -
./. - c.1476G>A 1476 r.(?) p.(=) - coding-synonymous -
./. - c.1476G>A 1476 r.(?) p.(=) - coding-synonymous -
./. - c.1476G>A 1476 r.(?) p.(=) - coding-synonymous -
./. - c.1476G>A 1476 r.(?) p.(=) - coding-synonymous -
./. - c.1476G>A 1476 r.(?) p.(=) - coding-synonymous -
./. - c.1476G>A 1476 r.(?) p.(=) - coding-synonymous -
./. - c.1476G>A 1476 r.(?) p.(=) - coding-synonymous -
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